Farmacovigilancia: Conceptos clave

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Crucigrama de términos de seguridad farmacéutica

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JORGE HERNAN OCAMPO CARDONA

Colombia

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Farmacovigilancia: Conceptos clave


Crucigrama Farmacovigilancia: Conceptos claveVersión en línea Crucigrama de términos de seguridad farmacéutica por JORGE HERNAN OCAMPO CARDONA 1 3-letter acronym: Drug-related problems 2 study the undesired effects 3 3-letter acronym for medicine-related problems. 4 science that studies the use of medicines 5 activity that identifies, evaluates and prevents the use of medications 6 any instrument used for the treatment or relief of a disease 7 study of the use of medications and their side effects in a large number of people 8 probability that a patient will experience an adverse reaction, injury, or unfavorable event 9 The ability of a drug to cause harm or unwanted adverse effects in a living organism 10 lack of expected response to a drug administered at doses appropriate for the approved indication 11 any unintended or unwanted effect of a drug that occurs at normal therapeutic doses, resulting from its own pharmacological action 12 Type B (unpredictable) immunologically mediated adverse drug reaction (ADR) that produces clinical symptoms following exposure to a drug in sensitized patients 13 Information reported about a possible new or incompletely documented causal relationship between a drug and an adverse event 14 any malfunction, alteration in the characteristics, performance, labeling or instructions for use of a medical device or drug that could or may have resulted in the death or serious deterioration of the health of the patient/user 15 absence of expected clinical response after administration of a drug, resulting in a lack of efficacy, often secondary to medication errors, patient factors (comorbidity), or biopharmaceutical problems 14 15 4 10 9 2 11 8 13 1 7 5 3 12 6 1 3-letter acronym: Drug-related problems 2 study the undesired effects 3 3-letter acronym for medicine-related problems. 4 science that studies the use of medicines 5 activity that identifies, evaluates and prevents the use of medications 6 any instrument used for the treatment or relief of a disease 7 study of the use of medications and their side effects in a large number of people 8 probability that a patient will experience an adverse reaction, injury, or unfavorable event 9 The ability of a drug to cause harm or unwanted adverse effects in a living organism 10 lack of expected response to a drug administered at doses appropriate for the approved indication 11 any unintended or unwanted effect of a drug that occurs at normal therapeutic doses, resulting from its own pharmacological action 12 Type B (unpredictable) immunologically mediated adverse drug reaction (ADR) that produces clinical symptoms following exposure to a drug in sensitized patients 13 Information reported about a possible new or incompletely documented causal relationship between a drug and an adverse event 14 any malfunction, alteration in the characteristics, performance, labeling or instructions for use of a medical device or drug that could or may have resulted in the death or serious deterioration of the health of the patient/user 15 absence of expected clinical response after administration of a drug, resulting in a lack of efficacy, often secondary to medication errors, patient factors (comorbidity), or biopharmaceutical problems 14 15 4 10 9 2 11 8 13 1 7 5 3 12 6

Farmacovigilancia: Conceptos clave

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Farmacovigilancia: Conceptos claveVersión en línea

por JORGE HERNAN OCAMPO CARDONA

3-letter acronym: Drug-related problems

study the undesired effects

3-letter acronym for medicine-related problems.

science that studies the use of medicines

activity that identifies, evaluates and prevents the use of medications

any instrument used for the treatment or relief of a disease

study of the use of medications and their side effects in a large number of people

probability that a patient will experience an adverse reaction, injury, or unfavorable event

The ability of a drug to cause harm or unwanted adverse effects in a living organism

lack of expected response to a drug administered at doses appropriate for the approved indication

any unintended or unwanted effect of a drug that occurs at normal therapeutic doses, resulting from its own pharmacological action

Type B (unpredictable) immunologically mediated adverse drug reaction (ADR) that produces clinical symptoms following exposure to a drug in sensitized patients

Information reported about a possible new or incompletely documented causal relationship between a drug and an adverse event

any malfunction, alteration in the characteristics, performance, labeling or instructions for use of a medical device or drug that could or may have resulted in the death or serious deterioration of the health of the patient/user

absence of expected clinical response after administration of a drug, resulting in a lack of efficacy, often secondary to medication errors, patient factors (comorbidity), or biopharmaceutical problems

3-letter acronym: Drug-related problems

study the undesired effects

3-letter acronym for medicine-related problems.

science that studies the use of medicines

activity that identifies, evaluates and prevents the use of medications

any instrument used for the treatment or relief of a disease

study of the use of medications and their side effects in a large number of people

probability that a patient will experience an adverse reaction, injury, or unfavorable event

The ability of a drug to cause harm or unwanted adverse effects in a living organism

lack of expected response to a drug administered at doses appropriate for the approved indication

any unintended or unwanted effect of a drug that occurs at normal therapeutic doses, resulting from its own pharmacological action

Type B (unpredictable) immunologically mediated adverse drug reaction (ADR) that produces clinical symptoms following exposure to a drug in sensitized patients

Information reported about a possible new or incompletely documented causal relationship between a drug and an adverse event

any malfunction, alteration in the characteristics, performance, labeling or instructions for use of a medical device or drug that could or may have resulted in the death or serious deterioration of the health of the patient/user

absence of expected clinical response after administration of a drug, resulting in a lack of efficacy, often secondary to medication errors, patient factors (comorbidity), or biopharmaceutical problems